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ABBOTT ARCHITECT FREE T4

K123379 Class II Special
Decision Date
2012-11-27
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K123379
Product Code CEC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1695
Decision Date 2012-11-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABBOTT ARCHITECT FREE T4 received FDA 510(k) clearance under submission number K123379, sponsored by Abbott Laboratories. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2012-11-27.

Classification & Regulation

This clearance is catalogued under FDA product code CEC and 21 CFR 862.1695, within the Clinical Chemistry review panel as a Class II device.